August 19, 2022 Pubblications
ABSTRACT
We present the case of an infant admitted to our department for a rapid broad complex tachycardia and cardi- ovascular collapse. The patient was submitted to genetic testing because of a conduction defect at baseline ECG and family history of gene mutation. A new SCN5A gene mutation variant was found leading to diagnosis of sodium-channel dysfunction arrhythmia.
Link to complete pubblication: https://www.techscience.com/chd/online/detail/18816
